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Human Genetics|April 10, 2025
The molecular landscape of hereditary ataxia: a single-center studyElisa Bregant, Elena Betto, Chiara Dal Secco, et al.
Frontiers in Neurology|March 15, 2024
Isolated insular stroke: topography is the answer with respect to outcome and cardiac involvementFedra Kuris, Sara Tartaglia, Roberto Sperotto, et al.
Neuromuscular Disorders : NMD|November 28, 2017
Identification and characterization of the novel m.8305C>T MTTK and m.4440G>A MTTM gene mutations causing mitochondrial myopathiesMauro Scarpelli, Lidia Carreño-Gago, Anna Russignan, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2026
Optimizing treatment for cervical dystonia: botulinum toxin alone or combined with physical therapy?Lorenzo Verriello, Fabrizio Bellizzi, Christian Lettieri, et al.
Neurobiology of Aging|March 12, 2018
Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patientsMerit Lamp, Paola Origone, Alessandro Geroldi, et al.
World Neurosurgery|January 22, 2023
Effect of Dexmedetomidine versus Propofol on Intraoperative Seizure Onset During Awake Craniotomy: A Retrospective StudyCristian Deana, Sara Pez, Tamara Ius, et al.
Neuroepidemiology|May 29, 2013
The incidence of amyotrophic lateral sclerosis in Friuli Venezia Giulia, Italy, from 2002 to 2009: a retrospective population-based studyDaniela Drigo, Lorenzo Verriello, Elena Clagnan, et al.
Neurobiology of Aging|April 13, 2010
Lack of association of PON polymorphisms with sporadic ALS in an Italian populationClaudia Ricci, Stefania Battistini, Lorena Cozzi, et al.
Journal of Neuro-Oncology|November 14, 2022
Performing real time neuropsychological testing during awake craniotomy: are dexmedetomidine or propofol the same? A preliminary reportBarbara Tomasino, Ilaria Guarracino, Giada Pauletto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 10, 2020
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypesMarcin M Machnicki, Valeria Guglielmi, Elia Pancheri, et al.
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